Variant report

Variant	nsv872547
Chromosome Location	chr1:172511969-172545832
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:184)
CpG islands
(count:306)
Chromatin interactive
region (count:64)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:184 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:172536592-172536681	K562	blood:	n/a	n/a
2	ARID3A	chr1:172526452-172526912	HepG2	liver:	n/a	chr1:172526750-172526766
3	ARID3A	chr1:172519144-172519422	K562	blood:	n/a	n/a
4	ATF3	chr1:172535369-172535700	K562	blood:	n/a	n/a
5	CCNT2	chr1:172520515-172520578	K562	blood:	n/a	n/a
6	CCNT2	chr1:172519174-172519339	K562	blood:	n/a	n/a
7	CEBPB	chr1:172525745-172525882	HepG2	liver:	n/a	n/a
8	CEBPB	chr1:172535330-172535652	HepG2	liver:	n/a	chr1:172535507-172535518
9	CEBPB	chr1:172525739-172525917	K562	blood:	n/a	n/a
10	CEBPB	chr1:172535319-172535704	K562	blood:	n/a	chr1:172535507-172535518
11	CEBPB	chr1:172535329-172535571	K562	blood:	n/a	chr1:172535507-172535518
12	CEBPB	chr1:172535283-172535703	K562	blood:	n/a	chr1:172535507-172535518
13	CEBPB	chr1:172535344-172535644	MCF-7	breast:	n/a	chr1:172535507-172535518
14	CEBPB	chr1:172535348-172535669	Hela-S3	cervix:	n/a	chr1:172535507-172535518
15	CEBPB	chr1:172535340-172535667	A549	lung:	n/a	chr1:172535507-172535518
16	CEBPB	chr1:172535366-172535612	H1-hESC	embryonic stem cell:	n/a	chr1:172535507-172535518
17	CEBPB	chr1:172535332-172535669	IMR90	lung:	n/a	chr1:172535507-172535518
18	CTCF	chr1:172514507-172514538	K562	blood:	n/a	n/a
19	CTCF	chr1:172537218-172537278	Medullo	brain:	n/a	n/a
20	CTCF	chr1:172515153-172515231	Fibrobl	skin:	n/a	n/a
21	CUX1	chr1:172514447-172514623	K562	blood:	n/a	n/a
22	CUX1	chr1:172517465-172517553	GM12878	blood:	n/a	n/a
23	EP300	chr1:172526432-172526787	HepG2	liver:	n/a	n/a
24	EP300	chr1:172536769-172536796	K562	blood:	n/a	n/a
25	EP300	chr1:172526409-172526842	HepG2	liver:	n/a	n/a
26	EP300	chr1:172544630-172544743	GM12878	blood:	n/a	n/a
27	FOXA1	chr1:172526339-172526903	HepG2	liver:	n/a	n/a
28	FOXA1	chr1:172526422-172526743	HepG2	liver:	n/a	n/a
29	FOXA1	chr1:172520196-172520481	T-47D	breast:	n/a	n/a
30	FOXA1	chr1:172526432-172526754	HepG2	liver:	n/a	n/a
31	FOXA1	chr1:172526352-172526883	HepG2	liver:	n/a	n/a
32	FOXA2	chr1:172526420-172526831	HepG2	liver:	n/a	n/a
33	FOXA2	chr1:172526380-172526922	HepG2	liver:	n/a	n/a
34	GATA1	chr1:172513235-172515173	PBDE	blood:	n/a	n/a
35	GATA2	chr1:172519100-172519300	SH-SY5Y	brain:	n/a	n/a
36	GATA3	chr1:172533035-172533287	MCF-7	breast:	n/a	n/a
37	GATA3	chr1:172514026-172514078	SH-SY5Y	brain:	n/a	n/a
38	GATA3	chr1:172519271-172519295	SH-SY5Y	brain:	n/a	n/a
39	GATA3	chr1:172530293-172530769	SK-N-SH	brain:	n/a	n/a
40	GATA3	chr1:172542867-172542987	SH-SY5Y	brain:	n/a	n/a
41	GATA3	chr1:172517673-172517717	SH-SY5Y	brain:	n/a	n/a
42	HNF4A	chr1:172526405-172526675	HepG2	liver:	n/a	n/a
43	IRF1	chr1:172529537-172529566	K562	blood:	n/a	n/a
44	IRF1	chr1:172514734-172515036	K562	blood:	n/a	n/a
45	IRF1	chr1:172516890-172517048	K562	blood:	n/a	n/a
46	IRF1	chr1:172514262-172514503	K562	blood:	n/a	n/a
47	IRF1	chr1:172527476-172527486	K562	blood:	n/a	n/a
48	IRF1	chr1:172520936-172521125	K562	blood:	n/a	n/a
49	IRF1	chr1:172520526-172521139	K562	blood:	n/a	chr1:172520609-172520623 chr1:172520599-172520613 chr1:172520605-172520619 chr1:172520603-172520617 chr1:172520603-172520613 chr1:172520609-172520619 chr1:172520601-172520621
50	IRF1	chr1:172527460-172527472	K562	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:172517922-172517972	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:172517922-172517972	HPAEpiC	pulmonary alveolar:	n/a
3	chr1:172517922-172517972	NHDF-neo	bronchial:	n/a
4	chr1:172540913-172540963	MCF10A-Er-Src	breast:	n/a
5	chr1:172543864-172543914	HL-60	blood:	n/a
6	chr1:172543864-172543914	NHDF-neo	bronchial:	n/a
7	chr1:172541012-172541062	HMEC	breast:	n/a
8	chr1:172543864-172543914	LNCaP	prostate:	n/a
9	chr1:172540913-172540963	HRE	kidney:	n/a
10	chr1:172515025-172515075	NT2-D1	testis:	n/a
11	chr1:172540913-172540963	HMEC	breast:	n/a
12	chr1:172541012-172541062	NB4	blood:	n/a
13	chr1:172540913-172540963	HCF	heart:	n/a
14	chr1:172515025-172515075	AG09309	skin:	n/a
15	chr1:172541012-172541062	AG10803	skin:	n/a
16	chr1:172515025-172515075	HepG2	liver:	n/a
17	chr1:172543864-172543914	HMEC	breast:	n/a
18	chr1:172540913-172540963	PANC-1	pancreas:	n/a
19	chr1:172543864-172543914	AG04449	skin:	fetal
20	chr1:172540913-172540963	MCF-7	breast:	n/a
21	chr1:172517922-172517972	GM12891	blood:	n/a
22	chr1:172515025-172515075	HNPCEpiC	eye:	n/a
23	chr1:172543864-172543914	PFSK-1	brain:	n/a
24	chr1:172541012-172541062	HCT-116	colon:	n/a
25	chr1:172517922-172517972	K562	blood:	n/a
26	chr1:172517922-172517972	SKMC	muscle:	n/a
27	chr1:172540913-172540963	NHDF-neo	bronchial:	n/a
28	chr1:172540913-172540963	HCPEpiC	choroid plexus:	n/a
29	chr1:172517922-172517972	HCPEpiC	choroid plexus:	n/a
30	chr1:172541012-172541062	Jurkat	blood:	n/a
31	chr1:172517922-172517972	AG09309	skin:	n/a
32	chr1:172541012-172541062	ECC-1	luminal epithelium:	n/a
33	chr1:172515025-172515075	HCF	heart:	n/a
34	chr1:172541012-172541062	NH-A	brain:	n/a
35	chr1:172515025-172515075	MCF10A-Er-Src	breast:	n/a
36	chr1:172543864-172543914	IMR90	lung:	fetal
37	chr1:172540913-172540963	Jurkat	blood:	n/a
38	chr1:172515025-172515075	HL-60	blood:	n/a
39	chr1:172541012-172541062	A549	lung:	n/a
40	chr1:172541012-172541062	SAEC	small airway:	n/a
41	chr1:172540913-172540963	K562	blood:	n/a
42	chr1:172540913-172540963	AoSMC	blood vessel:	n/a
43	chr1:172541012-172541062	MCF10A-Er-Src	breast:	n/a
44	chr1:172543864-172543914	HCM	heart:	n/a
45	chr1:172541012-172541062	IMR90	lung:	fetal
46	chr1:172515025-172515075	NH-A	brain:	n/a
47	chr1:172540913-172540963	GM12892	blood:	n/a
48	chr1:172543864-172543914	SK-N-SH_RA	brain:	n/a
49	chr1:172515025-172515075	LNCaP	prostate:	n/a
50	chr1:172541012-172541062	GM19239	blood:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:172524779..172527801-chr1:172528773..172532155,3	K562	blood:
2	chr1:172509695..172512146-chr1:172529892..172531866,2	K562	blood:
3	chr1:172524779..172527328-chr1:172528773..172530813,3	K562	blood:
4	chr1:172533299..172534999-chr1:172535109..172538092,2	K562	blood:
5	chr1:172520454..172524675-chr1:172533729..172536639,3	K562	blood:
6	chr1:172503233..172505429-chr1:172517362..172521428,4	MCF-7	breast:
7	chr1:172524779..172527801-chr1:172528773..172532155,3	K562	blood:
8	chr1:172520150..172522644-chr1:172528070..172530577,3	K562	blood:
9	chr1:172411247..172413190-chr1:172511240..172513810,2	MCF-7	breast:
10	chr1:172510611..172514641-chr1:172517107..172521407,5	K562	blood:
11	chr1:172509473..172512440-chr1:172512519..172514495,2	MCF-7	breast:
12	chr1:172530178..172532826-chr1:172534437..172536976,3	K562	blood:
13	chr1:172509473..172512440-chr1:172512519..172514495,2	MCF-7	breast:
14	chr1:172511443..172515146-chr1:172549683..172552996,3	K562	blood:
15	chr1:172527755..172529471-chr1:172533973..172536807,2	K562	blood:
16	chr1:172502047..172504329-chr1:172512042..172515759,3	MCF-7	breast:
17	chr1:172501396..172504430-chr1:172536696..172538886,3	MCF-7	breast:
18	chr1:172518787..172521238-chr1:172523963..172525755,2	MCF-7	breast:
19	chr1:172513266..172515531-chr1:172525208..172528046,2	K562	blood:
20	chr1:172500260..172503470-chr1:172516553..172520247,3	MCF-7	breast:
21	chr1:172530178..172532826-chr1:172534437..172536976,3	K562	blood:
22	chr1:172507308..172509751-chr1:172512083..172515617,3	K562	blood:
23	chr1:172418415..172420510-chr1:172512640..172515334,3	MCF-7	breast:
24	chr1:172418814..172420487-chr1:172526725..172528500,2	MCF-7	breast:
25	chr1:172524779..172527328-chr1:172528773..172530813,3	K562	blood:
26	chr1:172500449..172501968-chr1:172520222..172522221,2	K562	blood:
27	chr1:172530178..172532792-chr1:172534437..172536976,3	K562	blood:
28	chr1:172500667..172503739-chr1:172526545..172530565,4	K562	blood:
29	chr1:172410788..172413280-chr1:172514029..172516272,2	K562	blood:
30	chr1:172500340..172502764-chr1:172523653..172526492,2	K562	blood:
31	chr1:172500697..172503568-chr1:172528002..172531240,3	MCF-7	breast:
32	chr1:172499376..172501667-chr1:172538683..172540537,2	K562	blood:
33	chr1:172510611..172514641-chr1:172517107..172521407,5	K562	blood:
34	chr1:172518008..172521748-chr1:172521862..172526550,7	K562	blood:
35	chr1:172417587..172421346-chr1:172527795..172529688,3	MCF-7	breast:
36	chr1:172511128..172513343-chr1:172514678..172516974,2	K562	blood:
37	chr1:172542019..172544781-chr1:172548161..172550127,2	K562	blood:
38	chr1:172518787..172521238-chr1:172523963..172525755,2	MCF-7	breast:
39	chr1:172504989..172507379-chr1:172513184..172515018,2	MCF-7	breast:
40	chr1:172511128..172513343-chr1:172514678..172516974,2	K562	blood:
41	chr1:172501069..172504087-chr1:172524963..172528028,4	MCF-7	breast:
42	chr1:172410788..172413097-chr1:172513228..172515529,2	K562	blood:
43	chr1:172519187..172521470-chr1:172549104..172550723,2	K562	blood:
44	chr1:172417892..172422705-chr1:172522786..172525518,5	MCF-7	breast:
45	chr1:172518503..172521143-chr1:172524413..172526637,2	K562	blood:
46	chr1:172540565..172542685-chr1:172550671..172552538,2	K562	blood:
47	chr1:172499376..172501724-chr1:172539037..172541418,2	K562	blood:
48	chr1:172417853..172420301-chr1:172543266..172546052,2	MCF-7	breast:
49	chr1:172507927..172510625-chr1:172514126..172515983,2	MCF-7	breast:
50	chr1:172509695..172512146-chr1:172529892..172531866,2	K562	blood:

No data

Variant related genes	Relation type
SUCO	TF binding region
SUCO	CpG island
ENSG00000094975	chromatin interactions
ENSG00000180999	chromatin interactions
ENSG00000135845	chromatin interactions

Extended variants
information (count: 1176 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1176 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12087284	chr1:172511969-172511970	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544625148	chr1:172511978-172511979	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs563187671	chr1:172512050-172512051	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs367972572	chr1:172512083-172512084	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs533204796	chr1:172512091-172512092	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs544979700	chr1:172512109-172512110	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs560088427	chr1:172512174-172512175	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs527797500	chr1:172512180-172512181	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs376751927	chr1:172512191-172512192	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs116719536	chr1:172512261-172512262	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs148416057	chr1:172512281-172512282	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs142507323	chr1:172512284-172512285	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs74124232	chr1:172512292-172512293	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs571504915	chr1:172512296-172512297	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs376930295	chr1:172512313-172512314	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs74124233	chr1:172512382-172512383	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs553817417	chr1:172512411-172512412	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs565636447	chr1:172512416-172512417	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs115291158	chr1:172512451-172512452	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs554646280	chr1:172512508-172512509	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs140136938	chr1:172512614-172512615	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs189371286	chr1:172512633-172512634	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs556606542	chr1:172512640-172512641	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs180960508	chr1:172512725-172512726	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs369835061	chr1:172512728-172512729	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs72727516	chr1:172512733-172512734	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs565661528	chr1:172512791-172512792	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs111755666	chr1:172512797-172512798	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs561426651	chr1:172512816-172512817	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs531441977	chr1:172512818-172512819	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs577125915	chr1:172512837-172512838	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs546135722	chr1:172512899-172512900	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs536201736	chr1:172512937-172512938	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs532455482	chr1:172512959-172512960	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs530398968	chr1:172512968-172512969	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs562891692	chr1:172512980-172512981	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs547662676	chr1:172512986-172512987	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs59521518	chr1:172512991-172512992	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs554555981	chr1:172512999-172513000	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs140903652	chr1:172513003-172513004	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs149805616	chr1:172513059-172513060	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs373070534	chr1:172513119-172513120	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs201071815	chr1:172513124-172513125	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs569710163	chr1:172513127-172513128	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs553226622	chr1:172513335-172513336	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs536717760	chr1:172513361-172513362	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs542289859	chr1:172513363-172513364	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs12750740	chr1:172513444-172513445	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs577776461	chr1:172513447-172513448	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs370319694	chr1:172513468-172513469	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	20409316	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1182 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172503400-172528600	Weak transcription	Aorta	Aorta
2	chr1:172503400-172528600	Weak transcription	Lung	lung
3	chr1:172503600-172513600	Weak transcription	Psoas Muscle	Psoas
4	chr1:172503600-172520200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr1:172503600-172531600	Weak transcription	Esophagus	oesophagus
6	chr1:172503800-172529000	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr1:172503800-172534200	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr1:172504000-172524400	Weak transcription	HSMM	muscle
9	chr1:172504200-172515200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr1:172504200-172527000	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr1:172504400-172519400	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr1:172504800-172516200	Weak transcription	HUVEC	blood vessel
13	chr1:172505200-172518800	Weak transcription	Brain Angular Gyrus	brain
14	chr1:172505800-172519600	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr1:172506000-172512000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr1:172506000-172519000	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr1:172506000-172532600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr1:172506200-172525000	Weak transcription	Duodenum Mucosa	Duodenum
19	chr1:172506200-172526200	Weak transcription	Fetal Intestine Large	intestine
20	chr1:172506200-172528400	Weak transcription	Fetal Stomach	stomach
21	chr1:172507000-172516000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr1:172507200-172516800	Weak transcription	Brain Germinal Matrix	brain
23	chr1:172507200-172518400	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr1:172507400-172513000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr1:172507400-172513400	Weak transcription	K562	blood
26	chr1:172507400-172513800	Weak transcription	Stomach Mucosa	stomach
27	chr1:172507400-172515000	Weak transcription	Right Atrium	heart
28	chr1:172507400-172516400	Weak transcription	Brain Cingulate Gyrus	brain
29	chr1:172507400-172517600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr1:172507400-172518400	Weak transcription	NHEK	skin
31	chr1:172507400-172523000	Weak transcription	NHDF-Ad	bronchial
32	chr1:172507400-172526400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr1:172507400-172528600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr1:172507600-172512000	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr1:172507600-172512000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr1:172507600-172512200	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr1:172508000-172517400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr1:172508200-172513000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr1:172508200-172514400	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr1:172508200-172519200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr1:172508200-172526400	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr1:172508800-172515200	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr1:172509200-172512200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr1:172509200-172515600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr1:172509400-172513200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr1:172509400-172530800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr1:172509600-172514200	Weak transcription	Thymus	Thymus
48	chr1:172510000-172512200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr1:172510000-172512800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr1:172510000-172513400	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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